Sarah Scollon

2.8k total citations
47 papers, 991 citations indexed

About

Sarah Scollon is a scholar working on Genetics, Public Health, Environmental and Occupational Health and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Sarah Scollon has authored 47 papers receiving a total of 991 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Genetics, 11 papers in Public Health, Environmental and Occupational Health and 9 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Sarah Scollon's work include Genomics and Rare Diseases (17 papers), BRCA gene mutations in cancer (17 papers) and Childhood Cancer Survivors' Quality of Life (8 papers). Sarah Scollon is often cited by papers focused on Genomics and Rare Diseases (17 papers), BRCA gene mutations in cancer (17 papers) and Childhood Cancer Survivors' Quality of Life (8 papers). Sarah Scollon collaborates with scholars based in United States, Canada and Australia. Sarah Scollon's co-authors include Kami Wolfe Schneider, Barbara A. Bernhardt, Sharon E. Plon, Myra I. Roche, Denise Perry, Debra Skinner, Ashley N. Tomlinson, Laura M. Amendola, Harriet Druker and Wendy Kohlmann and has published in prestigious journals such as Journal of Clinical Oncology, Cancer and Cancer Research.

In The Last Decade

Sarah Scollon

43 papers receiving 977 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Sarah Scollon United States	17	473	267	199	193	178	47	991
Julie C. Sapp United States	22	757 1.6×	138 0.5×	563 2.8×	99 0.5×	157 0.9×	50	1.7k
Myra Wick United States	16	299 0.6×	170 0.6×	397 2.0×	139 0.7×	66 0.4×	55	1.1k
Jordan R. Hansford Australia	19	114 0.2×	133 0.5×	376 1.9×	139 0.7×	489 2.7×	65	1.4k
Cora M. Aalfs Netherlands	24	705 1.5×	263 1.0×	473 2.4×	144 0.7×	52 0.3×	81	1.9k
Jessica N. Everett United States	16	316 0.7×	82 0.3×	149 0.7×	89 0.5×	60 0.3×	30	985
Louise Izatt United Kingdom	19	587 1.2×	90 0.3×	449 2.3×	66 0.3×	42 0.2×	54	1.3k
Shanna Gustafson United States	12	290 0.6×	122 0.5×	95 0.5×	74 0.4×	24 0.1×	16	636
Kristen M. Shannon United States	19	771 1.6×	144 0.5×	342 1.7×	131 0.7×	29 0.2×	43	1.5k
Carolyn Russo United States	16	90 0.2×	168 0.6×	260 1.3×	133 0.7×	292 1.6×	31	1.1k
Daniel Satgé France	14	131 0.3×	109 0.4×	141 0.7×	201 1.0×	68 0.4×	42	557

Countries citing papers authored by Sarah Scollon

Since Specialization

Citations

This map shows the geographic impact of Sarah Scollon's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Sarah Scollon with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sarah Scollon more than expected).

Fields of papers citing papers by Sarah Scollon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sarah Scollon. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Sarah Scollon. The network helps show where Sarah Scollon may publish in the future.

Co-authorship network of co-authors of Sarah Scollon

This figure shows the co-authorship network connecting the top 25 collaborators of Sarah Scollon. A scholar is included among the top collaborators of Sarah Scollon based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Sarah Scollon. Sarah Scollon is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Lee, John H., Andrea Gilbert, Achint K. Singh, et al.. (2025). Anaplastic meningioma in a 6-year-old with somatic YAP1::MAML2 fusion and multiple endocrine neoplasia type 4 (MEN4) syndrome. Cancer Genetics. 292-293. 106–110. 1 indexed citations

Hansford, Jordan R., Anirban Das, Rose B. McGee, et al.. (2024). Update on Cancer Predisposition Syndromes and Surveillance Guidelines for Childhood Brain Tumors. Clinical Cancer Research. 30(11). 2342–2350. 9 indexed citations

Scollon, Sarah, Jill O. Robinson, Sabrina A. Suckiel, et al.. (2024). Satisfaction with mode of delivery of genomic sequencing results in a diverse national sample of research participants through the Clinical Sequencing Evidence-Generating Research Consortium. Genetics in Medicine. 26(9). 101176–101176.

Maese, Luke, Marcin W. Włodarski, Alison A. Bertuch, et al.. (2024). Update on Recommendations for Surveillance for Children with Predisposition to Hematopoietic Malignancy. Clinical Cancer Research. 30(19). 4286–4295. 3 indexed citations

Scollon, Sarah, et al.. (2024). A family-based approach to cascade genetic testing in a pediatric cancer genetics clinic. Familial Cancer. 24(1). 8–8.

Kamihara, Junne, Lisa Diller, William D. Foulkes, et al.. (2024). Neuroblastoma Predisposition and Surveillance—An Update from the 2023 AACR Childhood Cancer Predisposition Workshop. Clinical Cancer Research. 30(15). 3137–3143. 6 indexed citations

Michaeli, Orli, Marjolijn C.J. Jongmans, Jonathan D. Wasserman, et al.. (2024). Update on Cancer Screening in Children with Syndromes of Bone Lesions, Hereditary Leiomyomatosis and Renal Cell Carcinoma Syndrome, and Other Rare Syndromes. Clinical Cancer Research. 31(3). 457–465. 4 indexed citations

Zelley, Kristin, Jaclyn Schienda, Bailey Gallinger, et al.. (2024). Update on Genetic Counselor Practice and Recommendations for Pediatric Cancer Predisposition Evaluation and Surveillance. Clinical Cancer Research. 30(18). 3983–3989. 5 indexed citations

Gutierrez, Amanda M., Jill O. Robinson, Mary A. Majumder, et al.. (2023). Views of Adolescents and Young Adults with Cancer and Their Oncologists Toward Patients' Participation in Genomic Research. Journal of Adolescent and Young Adult Oncology. 12(5). 773–781. 2 indexed citations

10.

Scollon, Sarah, Jacquelyn Reuther, Ninad Patil, et al.. (2022). Distinct somatic DICER1 hotspot mutations in three metachronous ovarian Sertoli-Leydig cell tumors in a patient with DICER1 syndrome. Cancer Genetics. 262-263. 53–56.

11.

Bowling, Kevin M., Michelle L. Thompson, Melissa Kelly, et al.. (2022). Return of non-ACMG recommended incidental genetic findings to pediatric patients: considerations and opportunities from experiences in genomic sequencing. Genome Medicine. 14(1). 131–131. 10 indexed citations

12.

Scollon, Sarah, et al.. (2022). Evolution of germline TP53 variant classification in children with cancer. Cancer Genetics. 264-265. 29–32. 6 indexed citations

13.

Suckiel, Sabrina A., Julianne O’Daniel, Katie M. Gallagher, et al.. (2021). Genomic Sequencing Results Disclosure in Diverse and Medically Underserved Populations: Themes, Challenges, and Strategies from the CSER Consortium. Journal of Personalized Medicine. 11(3). 202–202. 6 indexed citations

14.

Reuther, Jacquelyn, Raghu Chandramohan, Horatiu Voicu, et al.. (2021). Genomic analysis and preclinical xenograft model development identify potential therapeutic targets for MYOD1 ‐mutant soft‐tissue sarcoma of childhood. The Journal of Pathology. 255(1). 52–61. 5 indexed citations

15.

Amendola, Laura M., Katie Golden‐Grant, & Sarah Scollon. (2021). Scaling Genetic Counseling in the Genomics Era. Annual Review of Genomics and Human Genetics. 22(1). 339–355. 20 indexed citations

16.

Gutierrez, Amanda M., Jill O. Robinson, Melody J. Slashinski, et al.. (2018). Agents of empathy: How medical interpreters bridge sociocultural gaps in genomic sequencing disclosures with Spanish-speaking families. Patient Education and Counseling. 102(5). 895–901. 16 indexed citations

17.

Lin, Frank Y., Katie Bergstrom, Richard Person, et al.. (2016). Integrated tumor and germline whole-exome sequencing identifies mutations in MAPK and PI3K pathway genes in an adolescent with rosette-forming glioneuronal tumor of the fourth ventricle. Molecular Case Studies. 2(5). a001057–a001057. 17 indexed citations

18.

Parsons, D. Williams, Angshumoy Roy, Federico A. Monzon, et al.. (2014). What’s in an exome? Diversity of diagnostic and incidental findings revealed by clinical tumor and germline sequencing of 100 children with solid tumors.. Journal of Clinical Oncology. 32(15_suppl). 10012–10012. 1 indexed citations

19.

Alderfer, Melissa A., Kristin Zelley, Robert B. Lindell, et al.. (2014). Parent decision‐making around the genetic testing of children for germline TP53 mutations. Cancer. 121(2). 286–293. 39 indexed citations

20.

Sugimura, Jun, Ximing J. Yang, Sarah Scollon, et al.. (2004). 747: Gene Expression Profiling of Chromophobe Renal Cell Carcinoma and Oncocytoma - Comparison and Identification of Novel Diagnostic Markers. The Journal of Urology. 171(4S). 198–198. 1 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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